FDA UDI In Commercial Distribution 🇺🇸 United States

IBEX Manual Refractor

DI: 00869228000465 · Model: MR · Trevi Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IBEX Manual Refractor
Primary DI
00869228000465
Version / Model
MR
Company Name
Trevi Technology, Inc.
Labeler DUNS
078605507
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-20
Public Version
1
Public Version Date
2023-01-30
Public Version Status
New
Public Device Record Key
e98193e2-6431-4a34-9c43-ba476b257e58

Device Description

Manual Refractor is an ophthalmic testing device used to measure an individual’s refractive error and determine their eyeglass prescription.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HKN Refractor, Manual, Non-Powered, Including Phoropter

GMDN Terms

Code Name
35299 Phoropter

Identifiers

Type ID
Primary 00869228000465

Customer Contacts

Phone
614-754-7175